Lowest-Energy Crystalline Polymorphs of P3HT

Andriy Zhugayevych, Olga Mazaleva, Artem Naumov, Sergei Tretiak

Research output: Contribution to journalArticlepeer-review

13 Citations (Scopus)


We systematically study low-energy crystalline polymorphs of the archetypal conjugated polymer, regioregular poly-3-hexylthiophene (rr-P3HT) using the best available density functional theory methods benchmarked against the ab initio coupled cluster method. A comprehensive conformational search is performed for two-dimensional π-stacks being the most rigid structural unit of bulk P3HT. We have identified a number of nearly isoenergetic polymorphs below the energy level of room-temperature amorphous structures and well below the energy of optimized best-fit experimental models. Classical molecular dynamics simulations show that these crystals retain their structure at least at 200 K. At room temperature, although the conjugated backbone of the π-stack remains ordered, aliphatic side chains are melted, transforming from low-energy folded conformations to high-entropy fully unfolded structures. Our study shows that P3HT is a statistically frustrated system with multiple competing interactions, which complicates fabrication of highly ordered bulk forms but gives structural flexibility of glasses.

Original languageEnglish
Pages (from-to)9141-9151
Number of pages11
JournalJournal of Physical Chemistry C
Issue number16
Publication statusPublished - 26 Apr 2018


Dive into the research topics of 'Lowest-Energy Crystalline Polymorphs of P3HT'. Together they form a unique fingerprint.

Cite this